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Article

VCP mutations are not a major cause of familial amyotrophic lateral sclerosis in the UK.

Journal of the neurological sciences - 15 Feb 2015

Kwok Chun Tak, Wang Hsiang-Ya, Morris Alex G, Smith Bradley, Shaw Christopher, de Belleroche Jackie

Abstract excerpt

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease causing loss of motor neurons in the spinal cord, brain stem and cerebral cortex. Mutations in the Valosin containing protein (VCP) gene have recently been identified in Familial ALS (FALS) patients, accounting for ~1% of all FALS...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 25618255
DOI: 10.1016/j.jns.2015.01.021

Genes

VCP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25618255-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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VCP mutations are not a major cause of familial amyotrophic lateral sclerosis in the UK.PMID 25618255Read ↗

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